The vinylogous Mukaiyama aldol reaction (VMAR) in natural product synthesis-Reference-Cited by-同舟云学术

The vinylogous Mukaiyama aldol reaction (VMAR) in natural product synthesis

Published:2014 Issue:4 Volume:31 Page:563-594
ISSN:0265-0568
Container-title:Nat. Prod. Rep.
language:en
Short-container-title:Nat. Prod. Rep.

Author:

Kalesse Markus¹²³⁴⁵,Cordes Martin¹²³,Symkenberg Gerrit¹²³,Lu Hai-Hua¹²³

Affiliation:

1. Institute for Organic Chemistry and Centre of Biomolecular Drug Research (BMWZ)

2. Leibniz Universität Hannover

3. 30167 Hannover, Germany

4. Helmholtz Centre for Infection Research (HZI)

5. Braunschweig, Germany

Abstract

This review will provide an overview on the recent developments of polyketide synthesis using the vinylogous Mukaiyama aldol reaction for the construction of advanced intermediates. In general, four different motifs can be constructed efficiently using the recent developments of asymmetric variants of this strategy.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/NP/C3NP70102F

Reference137 articles.

1. NEW ALDOL TYPE REACTION

2. The Principle of Vinylogy.

3. A CONVENIENT METHOD FOR THE PREPARATION OF δ-ALKOXY-α,β-UNSATURATED ALDEHYDES BY REACTION OF ACETALS WITH 1-TRIMETHYLSILOXY-1,3-BUTADIENE

4. Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products

5. Catalytic, Enantioselective, Vinylogous Aldol Reactions

Cited by 120 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Structure revision of lagunamide C to odoamide by total synthesis and biological evaluation;Tetrahedron;2024-03

2. Discovery of a nitroaromatic nannocystin with potent in vivo anticancer activity against colorectal cancer by targeting AKT1;Acta Pharmacologica Sinica;2024-02-07

3. The Aldol Reaction: Transition Metal Enolates;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

4. Electrophilic Fluorination of Silyl Dienol Ethers: a General and Selective Access to γ‐Fluoro Enals;Chemistry – A European Journal;2023-12-28

5. Synthesis of Spiro[4.5]ecanes by Au(I)‐Catalyzed Vinylogous Conia Ene Reaction;European Journal of Organic Chemistry;2023-12-14